亚热带茶园土壤的某些生物化学性状研究

茶园土壤的有机质含量、腐殖质组成、有机碳的循环与平衡特点、酶活性及其在施肥条件下的变化情况与土壤肥力密切相关．试验结果表明：亚热带茶园土壤有机质含量水平较低，腐殖质组成中以富里酸为主，HA／FA比、酶活性均比起源土壤略低；高产茶园土壤有机碳库的循环水平较高，在不施有机肥的情况下仍能保持平衡；低产茶园土壤有机碳库的循环水平较低，输出大于输入，施用有机肥可以较快地提高茶园土壤有机质含量和酶活性水平．增施有机肥和实行茶林复合是培肥茶园土壤、提高茶园生产力的有效措施．     

Mapping Soil Lead and Remediation Needs in Contaminated Soils

For the past two decades, the Taiwan Environmental Protection Administration has made a systematic investigation of As, Cd, Cr, Cu, Pb, Hg, Ni and Zn in agricultural soils to identify soil pollution from industrial production. The EPA has cooperated with local governmental agencies to establish a soil quality monitoring system that would upgrade the land recovery ability and prohibit polluted lands from being cultivated or turned over to other uses. Based on an island-wide soil survey, more than 1,000 hectares of arable soils in Taiwan were found to be considerably contaminated by heavy metals. One of the heavy metal contaminated sites, located near a ceramic product manufacturing factory in Nantou County, was identified as lead contaminated. According to the Nantou Environmental Protection Bureau, the lead content in contaminated sites showed a great variation of several mg Pbkg^–1 soil to several thousands mg Pbkg^–1 soil. Therefore, it is appropriate to estimate the lead spatial distribution through geostatistics such as Kriging. The soil lead concentration contour maps obtained by Kriging can help us to identify the pollution patterns and delineate the range of contaminated sites. The purpose of this study is to determine the Pb concentrations at each location by performing detailed soil sampling on those Pb contaminated sites and estimating the lead spatial distributions by Kriging. A total of 70 soils were sampled from different locations at two experiment sites. Lead contents were determined with 0.1M HCl extractable lead content of the soils. The results obtained by investigating the lead contents in each 15cm segment down to a 60cm depth, revealed that lead contents were greater in arable land near the ceramic products manufacturing factory, and lead concentrations decreased with depth. In addition, Pb concentrations in heavily contaminated soils showed heavy concentrations of Pb in specific locations. Results from Pb content spatial distributions indicated that the Kriging model is a useful tool and can provide decision-makers with critical information for delineating hazardous areas in heavy metal contaminated sites.     

表层土壤中有机污染物的光化学行为

本文首先简要介绍了光化学反应的基本原理。然后 ,重点介绍了研究表层土壤中有机污染物光化学行为的实验方法 ,影响光化学行为的因素及影响机理 ,光化学反应与吸附、迁移等的互相作用。最后阐述了这方面存在的问题 ,并且提出了一些建议     

Inorganic Ion Levels of Soils and Streams in some Areas of Ogoniland, Nigeria as Affected by Crude Oil Spillage

The inorganic ion concentrations of soils and streams in the three locations (Yorla, Zaakpon and Goi) in Ogoniland,Nigeria affected by crude oil spillage were investigated. In general, inorganic ion concentrations of polluted soilsand streams varied significantly (p = 0.05) from those of unpolluted soils and streams. Anions such as nitrate (NO ₃ ^- ), sulphate (SO ₄ ^2- ) and chloride(Cl^-) showed significantly (p = 0.05) higher values inthe polluted soils and steams than in the unpolluted controls. The phosphate (PO ₄ ^3- ) values were lowerin the polluted soils and streams than in the unpolluted controls.PO ₄ ^3- , NO ₃ ^- , SO ₄ ^2- and Cl^- concentrations were generally significantly (p = 0.05) higher in soils and streams from Yorla, Zaakpon and their control than in Goi North, Goi South and Goi control.Exchangeable cations and trace metal concentrations weresignificantly (p = 0.05) higher in the polluted soils andstreams than in the unpolluted controls. Yorla and Zaakponpolluted soils and streams had higher concentrations of theexchangeable cations and trace metals compared to valuesfrom Goi, except for Na. Results also showed significantlyhigher values of heavy metals (Pb, Cd, Cr and Ni) in the polluted soils compared to their controls, and values werealso significantly (p = 0.05) higher in Yorla, Zaakpon andtheir control compared to Goi North, Goi South and Goicontrol. Values obtained in polluted streams were higherthan in the unpolluted though not significant at the 5%level (p = 0.05). The anionic and cationic concentrationsof Yorla and Zaakpon soils and streams were generally higherthan those of Goi, indicating that Yorla and Zaakpon areaswere more polluted than Goi.Although the concentrations of most of the anions andcations analysed in the polluted soils and streams werewithin the World Health Organisation's permissible valuesfor the protection of humans and environment, the streams ofYorla, Zaakpon and Goi are in general being polluted withinorganic ions. This may make these soils and streamsunacceptable for domestic and industrial uses if not treated,and soils (farmlands) may also become unsuitable for agricultural purposes.     

京津唐地区土壤类型和水系分异对微量元素分布的影响分析

本文研究了不同土壤类型微量元素含量的差异,并对造成差异的因素进行了分析。 文中讨论了:1)京津唐地区土壤微量元素的背景含量;2)土壤微量元素含量与土壤类型的关系;3)土壤微量元素含量与水系的关系。     

A Simple Field Method to Determine Mercury Volatilization from Soils (3 pp)

Background Estimations of gaseous mercury volatilization from soils are often complex, stationary and expensive. Our objective was to develop a mobile and more simple, easy to handle and more cost-effective field method allowing rapid estimates of potential Hg emissions from soils. Methods. The study site is located in Germany, about 100 kilometers south-westerly of Berlin and influenced by the river Elbe and its tributary Saale river. The site is representative for a lot of other floodplain locations at the river Elbe and highly polluted with Hg and other heavy metals. For our study we developed a system consisting of a glass chamber gas, two gold traps, a battery operated pump and a gas meter. Adsorbed total gaseous mercury (TGM) in the gold traps was determined by use of atomic absorption spectrometry (AAS). Results and Discussion. In contrast to the common used flux chambers we designed a chamber without inlet and named it gas suck up chamber (GSC). TGM fluxes determined with the GSC showed a very close linear correlation (r = 0.993) between the TGM content in the gold traps and the corresponding pumped gas volume. The TGM adsorbed, increased proportional with increasing gas volume indicating homogenous concentrations of gaseous mercury in the soil air sucked. In contrast to the commonly used dynamic flux chamber with the aim of precisely measuring actual fluxes of Hg from a defined soil area, we focused on developing of a measurement system which will allow rapid estimates of potential Hg emissions of a site. Earlier research at the study site indicated a high potential for releasing volatile Hg from the soil to the atmosphere. Indeed, due to the high Hg content of the soil significant amounts of TGM could be detected and no shortage was reached. Conclusion. Our initial measurements are still too few in number neither to generalize the achieved results nor discuss controlling factors and processes. However, we are pleased to communicate that the developed GSC is well suited to become an effective sampling set up to rapidly estimate the magnitude of Hg volatilization from soils. Outlook. Further measurements at other polluted locations are necessary to verify the GSC method. In addition the use of a mercury analyzer instead of gold traps is planned for faster risk assessments.     

Distribution of PCDDs and PCDFs in Soils Collected from the Denver Front Range - Principal Components Analysis of Diffuse Dioxin Sources (10 pp)

Background, Aims and Scope The Rocky Mountain Arsenal (RMA) is a US Army facility located northeast of Denver, Colorado that has been listed on the National Priorities List (NPL). It is currently being re-mediated under the authority of the Comprehensive Environmental Response, Compensation, and Liability Act of 1980 (CERCLA) and the Superfund Amendments and Reauthorization Act of 1986 (SARA). As part of the remediation activities at RMA, indications were found that a source of polychlorinated dibenzo-p-dioxins (PCDDs) and polychlorinated dibenzofurans (PCDFs) had existed on the RMA. As a result, investigations were undertaken to assess the possible nature and extent of any potential sources of PCDDs and PCDFs on the RMA site. In addition, other studies were conducted that examined PCDD/PCDF contamination in the Denver area. The goal of these studies was to examine nature and extent of PCDD/PCDF contamination both on the RMA as well as in the surrounding Denver area. The intent of this study was to characterize sources of dioxins (PCDDs) and dibenzofurans (PCDFs) at low environmental concentrations which might have originated from diffuse sources in the Denver Colorado area and in particular, the Rocky Mountain Arsenal (RMA) using Principal Component Analysis (PCA). Methods Over 200 soil samples were collected from the RMA and the Denver area. From the RMA, soil was collected as part of three studies that included a (1) random site-wide sampling of the RMA, (2) soils from the Western Tier Parcel (WTP), and (3) soils from Historic Use areas. Denver area soil samples were collected from five different land use categories: Residential, Agricultural, Open Space, Commercial, and Industrial. PCA was conducted on concentrations of 17 2,3,7,8-substuituted PCDD and PCDF congeners in 220 soil samples collected from the RMA and the Denver Front Range region. Results and Discussion PCA demonstrated the presence of possible minor sources of dioxins on the RMA. Current remediation efforts on RMA will result in the removal of these sources. Samples from the RMA were identified by the presence of a congener profile containing higher chlorinated PCDFs while the Denver Front Range areas were characterized by the presence of higher chlorinated PCDD congeners. The presence of a PCDF signature for the RMA samples does not necessarily indicate a major source of these contaminants on-site. Indeed, the relatively diffuse nature of the sample clusters would argue strongly against the presence of a single large source. Instead, the predominance of the PCDF congeners probably indicates the mixed industrial activities that took place on and near the site. Conclusion PCA results indicate that PCDD/PCDF profiles in soils collected from the RMA differed from those collected from the outlying Denver areas but that a major source of these contaminants was not present. Rather, the diffuse nature of sample clusters from the PCA indicated that the congener profile of RMA samples was most likely a result of the mixed industrial activities that historically have taken place on and near the site. PCA also indicated that many of the 'open area' (peripheral site-wide) RMA soils samples did not differ from Denver are reference congener profiles. This finding was also true for samples collected from the WTP that were essentially indistinguishable from Off-RMA reference samples. In addition, total TEQ concentrations in soils collected from WTP were similar to those measured in soils collected from the Denver Front Range areas indicating that lack of a major source of PCDD/PCDF within the WTP zones of the RMA. Recommendation and Outlook Analytical as well as statistical results of the soil congener data indicate that the WTP soils are indistinguishable from soils collected from non-industrial areas in the Denver area. This finding would support the recent 'de-listing' of the WTP from the other RMA areas and its' transfer to other authorities in the Denver area.     

不同相伴阴离子对镉污染红壤微生物区系及群落功能多样性的影响

通过外加醋酸镉和氯化镉的室内培养试验研究了不同相伴阴离子对镉污染红壤中微生物区系及群落功能多样性的影响 .结果表明 :在相同镉浓度下相伴OAc-对镉污染红壤的细菌、放线菌和真菌数量及微生物群落功能多样性的抑制作用大于相伴Cl-.统计分析显示 ,在供试红壤中OAc-与Cl-对其微生物区系及微生物群落代谢剖面 (AWCD值 )、Shannon指数的影响均达到显著差异 (P <0 0 5 ) ,且在红砂土上表现更为明显 .外加醋酸钾和氯化钾的培养试验结果表明 ,阳离子为钾时 ,相伴OAc-与Cl-对红壤微生物区系结构及群落功能多样性没有产生明显抑制作用 ,相伴OAc-甚至存在一定的刺激作用 .可见 ,相伴OAc-对镉污染红壤微生物的毒害作用大于相伴Cl-,其原因并非是阴离子本身的毒性效应 ,而镉的生物有效性变化可能是不同相伴阴离子镉盐导致毒性差异的原因之一 .     

南京城市土壤Pb的含量及其化学形态

研究了南京城市土壤Pb的含量及其化学形态分布 ,结果表明 :土壤全Pb平均含量为 10 7 3mg kg ,变幅为 36 3— 472 6mg kg ,土壤Pb污染严重 .表层土壤Pb以残渣态和铁锰氧化物结合态为主 ,各形态比例为残渣态 >铁锰氧化物结合态 碳酸盐结合态 >有机结合态 >可交换态 .与非城区土壤比较 ,城市土壤中Pb不仅含量高 ,而且活性大 ,对环境危险性大     

东北三江平原土壤氧化CH4研究

三江平原土壤不同深度氧化大气浓度CH4和高浓度CH4的速率具有明显的垂直差异 .2个非淹水土壤整个剖面都具有氧化大气浓度CH4的潜力 ,以表层土的速率为最大 .非淹水的耕作土壤残留的有机质层仍保留了较强的氧化大气浓度CH4潜力 ,氧化CH4速率是耕作层的 2 0倍 .淹水土壤的大部分层次不具有氧化大气浓度CH4的潜力 .所有供试土壤均能消耗高浓度CH4,泥炭含量较高的土壤层次比矿质层氧化高浓度CH4的速率高